rs351771

Orientation

minus

Stabilized

minus

Make rs351771(C;C)

Make rs351771(C;T)

Make rs351771(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

112828864

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs351771
dbSNP (classic)	rs351771
ClinGen	rs351771
ebi	rs351771
HLI	rs351771
Exac	rs351771
Gnomad	rs351771
Varsome	rs351771
LitVar	rs351771
Map	rs351771
PheGenI	rs351771
Biobank	rs351771
1000 genomes	rs351771
hgdp	rs351771
ensembl	rs351771
geneview	rs351771
scholar	rs351771
google	rs351771
pharmgkb	rs351771
gwascentral	rs351771
openSNP	rs351771
23andMe	rs351771
SNPshot	rs351771
SNPdbe	rs351771
MSV3d	rs351771
GWAS Ctlg	rs351771

GMAF

0.3393

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 24078348] An Analysis of Polymorphisms Within the Wnt Signaling Pathway in Relation to Ovarian Cancer Risk in a Polish Population

[PMID 16569251] Single nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in Taiwan.

[PMID 18849522] Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes.

[PMID 20333795] APC gene mutations in Chinese familial adenomatous polyposis patients.

ClinVar
Risk	rs351771(T;T)
Alt	rs351771(T;T)
Reference	rs351771(C;C)
Significance	Other
Disease	not specified Familial colorectal cancer Hereditary cancer-predisposing syndrome APC-Associated Polyposis Disorders Familial adenomatous polyposis 1
Variation	info
Gene	APC
CLNDBN	not specified Familial colorectal cancer Hereditary cancer-predisposing syndrome APC-Associated Polyposis Disorders Familial adenomatous polyposis 1
Reversed	1
HGVS	NC_000005.9:g.112164561G>A
CLNSRC	ClinVar Emory University
CLNACC	RCV000035066.9, RCV000074153.1, RCV000162371.1, RCV000375983.1, RCV000411329.1,